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Recalls affecting Kansas

Data last updated: September 10, 2026 at 1:16 PM UTC

16,717 recalls found
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Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

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Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

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Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

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Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

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Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

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Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

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Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

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Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

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Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
Class IIModerate risk
DrugRecalled January 14, 2026

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11

Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0338-2026
Lot/product code:
Lots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
Recalling firm:
Amerisource Health Services LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 13, 2026

Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; 2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062; 3) LCSU 4, RTCA; Catalog Number: 881152;

Units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.

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FDA has not published a risk classification for this recall yet.

Recall #:
98039
Lot/product code:
1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; UDI-DI: 07045432088519; 2) LCSU 4, 300 ml, RTCA; Catalog Number: 880062; UDI-DI: 07045432088533; 3) LCSU 4, RTCA; Catalog Number: 881152; UDI-DI: 07045432067132;
Recalling firm:
Laerdal Medical Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 13, 2026

Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1

During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

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FDA has not published a risk classification for this recall yet.

Recall #:
98354
Lot/product code:
UDI-DI: 00763000543693; Lot Number: 0232837110, Additional lots as of 5/22/26: 0231547054 0231591827 0231758880 0231758898 0231758932 0231792414 0231792421 0231912903 0232670901 0232709219 0232709254 0232744928 0232784925 0232784989 0232805458
Recalling firm:
Medtronic Perfusion Systems
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/05;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 16-2840/05; UDI-DI: 04026575359240; Serial/Lot Number: 250513/2083, 250513/2085 , 250513/2086, 250513/2089, 250513/2090, 250513/2092, 250513/2093, 250513/2097 , 250513/2100, 250513/2102, 250513/2104, 250513/2107, 250513/2108, 251013/3245 , 251013/3247, 251013/3250, 251013/3251, 251013/3252, 251013/3253, 251105/0013 , 251105/0016, 251105/0018, 251105/0020, 251105/0032, 251105/0034, 251105/0036 , 251105/0037, 251105/0038, 251105/0039, 250513/2106, 250513/2099, 251105/0014 , 251105/0040, 251105/0002, 250513/2087, 250513/2091, 251013/3246, 251105/0019 , 251013/3249, 251105/0011, 251105/0012, 250513/2103, 250513/2105, 251013/3254;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/11;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-0027/11; UDI-DI: 04026575431953; Serial/Lot Number: 2549126, 2549127;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-8521/11;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-8521/11; UDI-DI: 04026575383245; Serial/Lot Number: 250728/2220, 250728/2222, 250728/2223, 250728/2224, 250728/2225, 250728/2226, 250728/2227;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/16;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-0027/16; UDI-DI: 04026575432134; Serial/Lot Number: 2550412, 2550413, 2549228;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-2835/12;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-2835/12; UDI-DI: 04026575316564; Serial/Lot Number: 241210/1809;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-8521/09;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-8521/09; UDI-DI: 04026575383238; Serial/Lot Number: 250728/0038, 250728/0039, 250728/0040, 250728/0041, 250728/0042, 250728/0043, 250728/0044, 250728/0045;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 16-2840/07; UDI-DI: 04026575359257; Serial/Lot Number: 250925/0480 , 250925/0481, 250925/0482, 250925/0483, 250925/0484, 250925/0486, 250925/0489 , 250925/0491, 250925/0492, 250925/0494, 250925/0503, 250925/0504, 250925/0345 , 250925/0346, 250925/0349, 250925/0350, 250925/0351, 250925/0352, 250925/0356 , 250925/0369, 250925/0501, 250925/0365, 250925/0368, 250925/0490, 250925/0488 , 250925/0479, 250925/0495, 250925/0500, 250925/0496, 250925/0499, 250925/0367;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-8030/12;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-8030/12; UDI-DI: 04026575048151; Serial/Lot Number: 250721/0194, 250721/0212, 250721/0211, 250721/0209;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-2836/11;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-2836/11; UDI-DI: 04026575316571; Serial/Lot Number: 250623/3643, 250623/3644, 250623/3645, 250623/3646, 250623/3648, 250812/2812, 250812/2811;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 16-2840/02; UDI-DI: 04026575359233; Serial/Lot Number: 250925/0640 , 250925/0641, 250925/0642, 250925/0646, 250925/0650, 250925/0652, 250925/0653 , 250925/0656, 250925/0658, 250925/0669, 250925/0670, 250925/0680, 250925/0681 , 250925/0682, 250925/0687, 250925/0689, 250925/0690, 250925/0691, 250925/0693 , 250925/0694, 251110/3293, 250925/0660, 250925/0661, 250925/0684, 250925/0685 , 250925/0657, 250925/0663, 250925/0659, 250925/0678, 251110/3288, 251110/3292 , 251110/3303, 251110/3313, 250925/0683, 250925/0674, 250925/0644, 250925/0665 , 250925/0668, 250925/0671, 250925/0673, 250925/0676, 250925/0664 , 250925/0651 , 251110/3297, 251110/3289, 250925/0639, 250925/0648, 250925/0688, 250925/0696;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/15;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-0027/15; UDI-DI: 04026575432127; Serial/Lot Number: 2549190;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/12;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-0027/12; UDI-DI: 04026575431960; Serial/Lot Number: 2549036;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 12, 2026

Endo-Model Replacement Plateau; Item Number: 15-8521/15;

The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98342
Lot/product code:
Item Number: 15-8521/15; UDI-DI: 04026575383283; Serial/Lot Number: 250805/0020, 250805/0021, 250805/0023, 250805/0024;
Recalling firm:
Waldemar Link GmbH & Co. KG (Mfg Site)
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled January 10, 2026

Furosemide Tablets, USP 40 mg, 1,000 Tablets, Rx Only, Manufactured for: Rising Pharmaceuticals Inc., East Brunswick, NJ 08816, Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, India, NDC 64980-563-10.

Presence of Foreign Substance

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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0293-2026
Lot/product code:
Lot# FUB125042G; Exp. 05/13/2027
Recalling firm:
Graviti Pharmaceuticals Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1102-2026
Lot/product code:
Product Number SMBARPD20001 Batch/Lot 025233 and Use By 08/31/2026 Batch/Lot 025237 and Use By 08/31/2026 Batch/Lot 025238 and Use By 08/31/2026 Batch/Lot 025239 and Use By 08/31/2026 Batch/Lot 025240 and Use By 08/31/2026 Batch/Lot 025241 and Use By 08/31/2026 Batch/Lot 025261 and Use By 09/30/2026 Batch/Lot 025265 and Use By 09/30/2026 Batch/Lot 025267 and Use By 09/30/2026 Batch/Lot 025268 and Use By 09/30/2026 Batch/Lot 025290 and Use By 10/31/2026 Batch/Lot 025294 and Use By 10/31/2026 Batch/Lot 025329 and Use By 11/30/2026 Batch/Lot 025330 and Use By 11/30/2026 Batch/Lot 025339 and Use By 12/31/2026 Batch/Lot 025343 and Use By 12/31/2026
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1097-2026
Lot/product code:
Product Number SMBARMB20001 Batch/Lot 025220 and Use By 08/31/2026 Batch/Lot 025223 and Use By 08/31/2026 Batch/Lot 025247 and Use By 09/30/2026 Batch/Lot 025248 and Use By 09/30/2026 Batch/Lot 025251 and Use By 09/30/2026 Batch/Lot 025253 and Use By 09/30/2026 Batch/Lot 025275 and Use By 10/31/2026 Batch/Lot 025281 and Use By 10/31/2026 Batch/Lot 025288 and Use By 10/31/2026 Batch/Lot 025296 and Use By 10/31/2026 Batch/Lot 025335 and Use By 12/31/2026 Batch/Lot 025337 and Use By 12/31/2026 Batch/Lot 026008 and Use By 01/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only). 2) Spring & Mulberry Pure Dark Minis Date-Sweetened Chocolate, Net Wt. 0.75 oz. (22g), individually packaged in a navy blue box, UPC 850055470132, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 64 bars (caddied)/204 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

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▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1103-2026
Lot/product code:
1) Pure Dark: Product Number SMBARPC20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025218 and Use By 02/28/2027 Batch/Lot 025219 and Use By 02/28/2027 Batch/Lot 025254 and Use By 03/31/2027 Batch/Lot 025266 and Use By 03/31/2027 Batch/Lot 025269 and Use By 03/31/2027 Batch/Lot 025324 and Use By 05/31/2027 Batch/Lot 025338 and Use By 06/30/2027 Batch/Lot 025350 and Use By 06/30/2027 2) Pure Dark Minis: Product Number SMBARPC30001 Batch/Lot 025273 and Use By 03/31/2027 Batch/Lot 025302 and Use By 04/30/2027 Batch/Lot 025303 and Use By 04/30/2027 Batch/Lot 026009 and Use By 07/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 9, 2026

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98353
Lot/product code:
Lot Code: Version or Model: A-5750.16/1 Device Description: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Lot: 25472432
Recalling firm:
Medartis AG
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 9, 2026

Diowave Laser System, REF: Diowave 250W

Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98507
Lot/product code:
UDI-DI: G180DIOWAVESTEALTHMAX0. All software versions prior to, but not including V1.81
Recalling firm:
Technological Medical Advancements LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1099-2026
Lot/product code:
Product Number SMBARLR20001 Batch/Lot 025204 and Use By 01/31/2027 Batch/Lot 025205 and Use By 01/31/2027 Batch/Lot 025212 and Use By 02/28/2027 Batch/Lot 025216 and Use By 02/28/2027 Batch/Lot 025259 and Use By 03/31/2027 Batch/Lot 025260 and Use By 03/31/2027 Batch/Lot 026037 and Use By 08/31/2027 Batch/Lot 026040 and Use By 08/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

Spring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1096-2026
Lot/product code:
Product Number SMBARML20001 Batch/Lot 025225 and Use By 02/28/2027 Batch/Lot 025255 and Use By 03/31/2027 Batch/Lot 025272 and Use By 03/31/2027 Batch/Lot 025342 and Use By 06/30/2027 Batch/Lot 025364 and Use By 06/30/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusSalmonellaRecalled January 9, 2026

Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1104-2026
Lot/product code:
Product Number SMBARSS20001 Batch/Lot 026013 and Use By 07/31/2027 Batch/Lot 026014 and Use By 07/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)